Method for manufacturing high-strength galvanized steel sheet

ABSTRACT

A method for manufacturing a high-strength galvanized steel sheet having excellent strength-elongation balance, coating adhesiveness, and surface appearance. The method includes: (i) a first heating process of heating a steel sheet having a predetermined chemical composition, (ii) a first pickling process of pickling the steel sheet which was subjected to the first heating process in an oxidizing acidic aqueous solution, (iii) a second pickling process of pickling the steel sheet which was subjected to the first pickling process in a non-oxidizing acidic aqueous solution, (iv) a second heating process of holding the steel sheet, which was subjected to the second pickling process, at a temperature range of 700° C. or higher and 900° C. or lower in a hydrogen-containing atmosphere for 20 seconds or more and 300 seconds or less, and (v) performing a galvanizing treatment on the steel sheet which was subjected to the second heating process.

TECHNICAL FIELD

This application relates to a method for manufacturing a high-strength galvanized steel sheet which can preferably be used for automobile members.

BACKGROUND

Nowadays, there is a strong demand for improving fuel efficiency to reduce the amount of CO₂ emissions from automobiles from the viewpoint of global environment conservation. In response to such a demand, since there is an active trend toward decreasing the thickness of automobile body parts to reduce the weight of automobile bodies, there is an increasing need for increasing the strength of a steel sheet, which is a material for automobile body parts.

To increase the strength of a steel sheet, adding solid solution-strengthening elements, such as Si and Mn, is effective. However, since such elements are easily oxidizable elements, which are oxidized more readily than Fe, the following problems exist in the case where a galvanized steel sheet or a galvannealed steel sheet whose base steel is a high-strength steel sheet containing large amounts of such elements is manufactured.

Usually, to manufacture a galvanized steel sheet, a galvanizing treatment is performed after a steel sheet is subjected to heating and annealing at a temperature of approximately 600° C. to 900° C. in a non-oxidizing atmosphere or in a reducing atmosphere. Easily oxidizable elements in steel are selectively oxidized even in a non-oxidizing atmosphere or a reducing atmosphere, which is generally used, and concentrated on the surface of a steel sheet to form oxides on the surface. Since such oxides deteriorate wettability between the surface of the steel sheet and molten zinc when a galvanizing treatment is performed, there is a rapid deterioration in coating wettability with an increase in the concentration of easily oxidizable elements in steel, which results in frequent non-coating occurring. Even in the case where non-coating does not occur, since oxides exist between a steel sheet and a coating layer, there is a deterioration in coating adhesiveness. In particular, since only a small amount of Si added markedly deteriorates the wettability with molten zinc, Mn, whose effect on wettability is less than that of Si, is added in many cases when a galvanized steel sheet is manufactured. However, since Mn oxides also deteriorate the wettability with molten zinc, the problem of non-coating becomes marked in the case where a large amount of Mn is added.

In response to such problems, Patent Literature 1 proposes a method in which, after annealing has been performed on a steel sheet, pickling is performed to dissolve and remove oxides formed on the surface of the steel sheet, annealing is thereafter performed again, and a galvanizing treatment is performed. However, when this method is used in the case where large amounts of alloy elements are added, since oxides are formed on the surface of the steel sheet again when annealing is performed again, there may be a deterioration in coating adhesiveness even in the case where surface appearance defects, such as non-coating, do not occur.

Examples of a method for improving coating adhesiveness include one in which minute asperity is formed on the surface of a steel sheet to achieve an anchor effect at a coating interface. Patent Literature 2 proposes a method in which sphere-shaped or massive Mn oxides, which are formed on the surface of a Mn-containing steel sheet after the steel sheet has been annealed, are pressed onto the surface of the steel sheet by performing rolling and then removed by performing pickling to form minute asperity on the surface of the steel sheet. However, in the case of this method, it is necessary to add a rolling process after an annealing process. Moreover, although this method is effective in the case of steel containing Mn, which is likely to form sphere-shaped or massive oxides after annealing has been performed, this method is less effective in the case of high-Si-containing steel, which is likely to form film-shaped oxides. In addition, since it is difficult to remove Si oxides in a subsequent pickling process due to poor reactivity thereof, the upper limit of the acceptable amount of Si added is comparatively small, that is, 0.80%, which is not sufficient to achieve the effect of achieving an excellent strength-elongation balance caused by adding Si.

CITATION LIST Patent Literature

PTL 1: Japanese Patent No. 3956550

PTL 2: Japanese Patent Application No. 2015-551886

SUMMARY Technical Problem

In view of the situation described above, an object of the disclosed embodiments is to provide a method for manufacturing a high-strength galvanized steel sheet excellent in terms of strength-elongation balance, coating adhesiveness, and surface appearance.

Solution to Problem

The present inventors diligently conducted investigations and studies to solve the problems described above and, as a result, found that, by performing annealing, pickling in an oxidizing aqueous solution, rinsing in water, pickling in a non-oxidizing aqueous solution, and rinsing in water in this order on Si-containing steel, since Si oxides formed on the surface of the steel are removed along with the base steel grains, it is possible to achieve a clean steel sheet surface, which makes it possible to perform a galvanizing treatment on the surface of the steel sheet after subsequent second annealing has been performed. It was found that, since this makes it possible to use a material design involving two annealing processes even in the case of Si-containing steel, it is possible to manufacture a galvanized steel sheet excellent in terms of strength (TS)-elongation (El) balance. Moreover, it was found that, as an additional effect, since minute asperity is formed on the surface of a steel sheet which has been pickled in an oxidizing aqueous solution, there is an improvement in coating adhesiveness due to an anchor effect at a coating interface after galvanizing treatment has been performed.

The disclosed embodiments have been made on the basis of the knowledge described above, and the exemplary embodiments are as follows.

[1] A method for manufacturing a high-strength galvanized steel sheet, the method including a first heating process of heating a steel sheet having a chemical composition containing, by mass %, C: 0.040% or more and 0.500% or less, Si: 0.80% or more and 2.00% or less, Mn: 1.00% or more and 4.00% or less, P: 0.100% or less, S: 0.0100% or less, Al: 0.100% or less, N: 0.0100% or less, and a balance of Fe and inevitable impurities to a temperature range of 800° C. or higher and 950° C. or lower in an atmosphere having a H₂ concentration of 0.05 vol % or more and 30.0 vol % or less and a dew point of 0° C. or lower, a first pickling process of pickling the steel sheet which has been subjected to the first heating process in an oxidizing acidic aqueous solution and of rinsing the pickled steel sheet in water, a second pickling process of pickling the steel sheet which has been subjected to the first pickling process in a non-oxidizing acidic aqueous solution and of rinsing the pickled steel sheet in water, a second heating process of holding the steel sheet which has been subjected to the second pickling process in a temperature range of 700° C. or higher and 900° C. or lower in an atmosphere having a H₂ concentration of 0.05 vol % or more and 30.0 vol % or less and a dew point of 0° C. or lower for 20 seconds or more and 300 seconds or less, and a process of performing a galvanizing treatment on the steel sheet which has been subjected to the second heating process.

[2] The method for manufacturing a high-strength galvanized steel sheet according to item [1], in which the chemical composition further contains, by mass %, at least one selected from Ti: 0.010% or more and 0.100% or less, Nb: 0.010% or more and 0.100% or less, and B: 0.0001% or more and 0.0050% or less.

[3] The method for manufacturing a high-strength galvanized steel sheet according to item [1] or [2], in which the chemical composition further contains, by mass %, at least one selected from Mo: 0.01% or more and 0.50% or less, Cr: 0.60% or less, Ni: 0.50% or less, Cu: 1.00% or less, V: 0.500% or less, Sb: 0.10% or less, Sn: 0.10% or less, Ca: 0.0100% or less, and REM: 0.010% or less.

[4] The method for manufacturing a high-strength galvanized steel sheet according to any one of items [1] to [3], the method further including an oxidizing process of heating the steel sheet to a temperature range of 400° C. or higher and 900° C. or lower in an atmosphere having an O₂ concentration of 0.1 vol % or more and 20 vol % or less and a H₂O concentration of 1 vol % or more and 50 vol % or less after the second pickling process and before the second heating process.

[5] The method for manufacturing a high-strength galvanized steel sheet according to item [4], the method further including a reducing process of heating the steel sheet to a temperature range of 600° C. or higher and 900° C. or lower in an atmosphere having an O₂ concentration of 0.01 vol % or more and less than 0.1 vol % and a H₂O concentration of 1 vol % or more and 20 vol % or less after the oxidizing process.

[6] The method for manufacturing a high-strength galvanized steel sheet according to any one of items [1] to [5], in which the oxidizing acidic aqueous solution in the first pickling process is nitric acid or a mixture of nitric acid and at least one selected from hydrochloric acid, hydrofluoric acid, and sulfuric acid.

[7] The method for manufacturing a high-strength galvanized steel sheet according to any one of items [1] to [6], in which the non-oxidizing acidic aqueous solution in the second pickling process is a mixture of one, two, or more selected from hydrochloric acid, sulfuric acid, phosphoric acid, pyrophosphoric acid, formic acid, acetic acid, citric acid, hydrofluoric acid, and oxalic acid.

[8] The method for manufacturing a high-strength galvanized steel sheet according to any one of items [1] to [7], the method further including an alloying treatment process of performing an alloying treatment on the steel sheet which has been subjected to the process of performing a galvanizing treatment.

Advantageous Effects

According to the disclosed embodiments, it is possible to obtain a high-strength galvanized steel sheet excellent in terms of strength-elongation balance, surface appearance, and coating adhesiveness. By using the high-strength galvanized steel sheet according to the disclosed embodiments for, for example, the structural members of automobiles, it is possible to improve fuel efficiency due to weight reduction of automobile bodies.

DETAILED DESCRIPTION

Hereafter, the embodiments of the present application will be described. Here, the present application is not limited to the embodiments below. In addition, “%” used when describing a chemical composition refers to “mass %”.

First, the chemical composition will be described. The chemical composition contains, by mass %, C: 0.040% or more and 0.500% or less, Si: 0.80% or more and 2.00% or less, Mn: 1.00% or more and 4.00% or less, P: 0.100% or less, S: 0.0100% or less, Al: 0.100% or less, and N: 0.0100% or less, and the balance is Fe and inevitable impurities. In addition, the chemical composition may further contain, at least one selected from Ti: 0.010% or more and 0.100% or less, Nb: 0.010% or more and 0.100% or less, and B: 0.0001% or more and 0.0050% or less. In addition, the chemical composition may further contain, at least one selected from Mo: 0.01% or more and 0.50% or less, Cr: 0.60% or less, Ni: 0.50% or less, Cu: 1.00% or less, V: 0.500% or less, Sb: 0.10% or less, Sn: 0.10% or less, Ca: 0.0100% or less, and REM: 0.010% or less. Hereafter, each of the constituents will be described.

C: 0.040% or More and 0.500% or Less

C is an element which stabilizes austenite and which is effective for improving strength and ductility. To achieve such effects, the C content is set to be 0.040% or more. On the other hand, in the case where the C content is more than 0.500%, there is a marked deterioration in weldability, and there may be a case where it is not possible to achieve an excellent strength-elongation balance due to an excessively hardened martensite phase. Therefore, the C content is set to be 0.500% or less.

Si: 0.80% or More and 2.00% or Less

Si is an element which stabilizes ferrite. Si is also effective for increasing the strength of steel through solid solution strengthening, and improves strength-elongation balance. In the case where the Si content is less than 0.80%, it is not possible to achieve such effects. On the other hand, in the case where the Si content is more than 2.00%, since Si forms oxides on the surface of a steel sheet during annealing, there is a deterioration in wettability between the steel sheet and molten zinc when galvanizing is performed, which results in the occurrence of surface appearance defects, such as non-coating. Therefore, the Si content is set to be 0.80% or more and 2.00% or less.

Mn: 1.00% or More and 4.00% or Less

Mn is an element which stabilizes austenite and which is effective for achieving satisfactory strength of an annealed steel sheet. To achieve such strength, the Mn content is set to be 1.00% or more. However, in the case where the Mn content is more than 4.00%, since Mn forms a large amount of oxides on the surface of a steel sheet during annealing, there is a deterioration in wettability between the steel sheet and molten zinc when galvanizing is performed, which may result in surface appearance defects. Therefore, the Mn content is set to be 4.00% or less.

P: 0.100% or Less

P is an element which is effective for increasing the strength of steel. From the viewpoint of increasing the strength of steel, it is preferable that the P content be 0.001% or more. However, in the case where the P content is more than 0.100%, since embrittlement occurs due to grain boundary segregation, there is a deterioration in impact resistance. In addition, in the case where an alloying treatment is performed after a galvanizing treatment has been performed, an alloying reaction may be delayed. Therefore, the P content is set to be 0.100% or less.

S: 0.0100% or Less

S forms inclusions, such as MnS, which results in a deterioration in impact resistance and results in cracking occurring along a metal flow in a weld zone. Therefore, it is preferable that the S content be as small as possible, and, thereby, the S content is set to be 0.0100% or less.

Al: 0.100% or Less

In the case where the Al content is excessively large, there is a deterioration in surface quality and formability due to an increase in the amount of oxide-based inclusions. In addition, there is an increase in cost. Therefore, the Al content is set to be 0.100% or less. It is preferable that the Al content be 0.050% or less.

N: 0.0100% or Less

Since N is an element which deteriorates the aging resistance of steel, it is preferable that the N content be as small as possible. In the case where the N content is more than 0.0100%, there is a marked deterioration in aging resistance. Therefore, the N content is set to be 0.0100% or less.

Remainder is Fe and inevitable impurities. Here, the high-strength galvanized steel sheet according to the disclosed embodiments may contain the elements below as needed for the purpose of, for example, increasing strength.

Ti: 0.010% or More and 0.100% or Less

Ti is an element which contributes to increasing the strength of a steel sheet by combining with C or N to form fine carbides or fine nitrides in the steel sheet. To achieve such an effect, it is preferable that the Ti content be 0.010% or more. On the other hand, in the case where the Ti content is more than 0.100%, such an effect becomes saturated. Therefore, it is preferable that the Ti content be 0.100% or less.

Nb: 0.010% or More and 0.100% or Less

Nb is an element which contributes to increasing strength through solid solution strengthening or precipitation strengthening. To achieve such an effect, it is preferable that the Nb content be 0.010% or more. On the other hand, in the case where the Nb content is more than 0.100%, since there is a deterioration in the ductility of a steel sheet, there may be a deterioration in workability. Therefore, it is preferable that the Nb content be 0.100% or less.

B: 0.0001% or More and 0.0050% or Less

B is an element which contributes to increasing the strength of a steel sheet by improving hardenability. To achieve such an effect, it is preferable that the B content be 0.0001% or more. On the other hand, in the case where the B content is excessively large, since there is a deterioration in ductility, there may be a deterioration in workability. In addition, in the case where the B content is excessively large, there is also an increase in cost. Therefore, it is preferable that the B content be 0.0050% or less.

Mo: 0.01% or More and 0.50% or Less

Mo is an element which forms austenite and which is effective for achieving satisfactory strength of an annealed steel sheet. From the viewpoint of achieving satisfactory strength, it is preferable that the Mo content be 0.01% or more. However, since Mo incurs increased alloy costs, there is an increase in cost in the case where the Mo content is large. Therefore, it is preferable that the Mo content be 0.50% or less.

Cr: 0.60% or Less

Cr is an element which forms austenite and which is effective for achieving satisfactory strength of an annealed steel sheet. To achieve such effects, it is preferable that the Cr content be 0.01% or more. On the other hand, in the case where the Cr content is more than 0.60%, there may be a deterioration in the surface appearance of a coating layer due to oxides being formed on the surface of a steel sheet during annealing. Therefore, it is preferable that the Cr content be 0.60% or less.

Ni: 0.50% or Less, Cu: 1.00% or Less, and V: 0.500% or Less

Ni, Cu, and V are elements which are effective for increasing the strength of steel and which may be used to increase the strength of steel within the ranges according to the disclosed embodiments. To increase the strength of steel, it is preferable that the Ni content be 0.05% or more, that the Cu content be 0.05% or more, and that the V content be 0.005% or more. However, in the case where the Ni content is more than 0.50%, the Cu content is more than 1.00%, or the V content is more than 0.500% because of an excessive addition, there may be a deterioration in ductility due to a marked increase in strength. In addition, in the case where the contents of these elements are excessively large, there is also an increase in cost. Therefore, in the case where these elements are added, it is preferable that the Ni content be 0.50% or less, that the Cu content be 1.00% or less, and that the V content be 0.500% or less.

Sb: 0.10% or Less and Sn: 0.10% or Less

Sb and Sn have a function of inhibiting nitriding in the vicinity of the surface of a steel sheet. To inhibit nitriding, it is preferable that the Sb content be 0.005% or more and that the Sn content be 0.005% or more. However, in the case where the Sn content is more than 0.10% or the Sb content is more than 0.10%, the effect described above becomes saturated. Therefore, in the case where these elements are added, it is preferable that the Sb content be 0.10% or less and that the Sn content be 0.10% or less.

Ca: 0.0100% or Less

Ca is effective for improving ductility by controlling the shape of sulfides, such as MnS. To achieve such an effect, it is preferable that the Ca content be 0.0010% or more. However, in the case where the Ca content is more than 0.0100%, the effect described above becomes saturated. Therefore, in the case where Ca is added, it is preferable that the Ca content be 0.0100% or less.

REM: 0.010% or Less

REM contributes to improving workability by controlling the shape of sulfide-based inclusions. To achieve the effect of improving workability, it is preferable that the REM content be 0.001% or more. In addition, in the case where the REM content is more than 0.010%, since there is an increase in the amount of inclusions, there may be a deterioration in workability. Therefore, in the case where REM is added, it is preferable that the REM content be 0.010% or less.

Hereafter, the method for manufacturing the high-strength galvanized steel sheet according to the disclosed embodiments will be described.

A steel slab having the chemical composition described above is subjected to rough rolling and finish rolling in a hot rolling process, and cold rolling is performed after scale formed on the surface layer of the hot-rolled steel sheet has been removed in a pickling process. Here, there is no particular limitation on the conditions applied for the hot rolling process, the pickling process, or the cold rolling process, and the conditions may be appropriately determined. In addition, all or part of the hot rolling process may be omitted by using, for example, a thin-slab casting method.

Subsequently, the processes below, which relate to the important features of the disclosed embodiments, are performed.

A first heating process of heating a steel sheet to a temperature range of 800° C. or higher and 950° C. or lower in an atmosphere having a H₂ concentration of 0.05 vol % or more and 30.0 vol % or less and a dew point of 0° C. or lower, a first pickling process of pickling the steel sheet which has been subjected to the first heating process in an oxidizing acidic aqueous solution and of rinsing the pickled steel sheet in water, a second pickling process of pickling the steel sheet which has been subjected to the first pickling process in a non-oxidizing acidic aqueous solution and of rinsing the pickled steel sheet in water, a second heating process of holding the steel sheet which has been subjected to the second pickling process in a temperature range of 700° C. or higher and 900° C. or lower in an atmosphere having a H₂ concentration of 0.05 vol % or more and 30.0 vol % or less and a dew point of 0° C. or lower for 20 seconds or more and 300 seconds or less, and a process of performing a galvanizing treatment on the steel sheet which has been subjected to the second heating process are performed. Here, the processes described above may be performed in a continuous line, or a separate line may be used for each of the processes.

Hereafter, the processes will be described in detail.

First Heating Process

The first heating process is a process in which the steel sheet described above is heated to a temperature range of 800° C. or higher and 950° C. or lower in an atmosphere having a H₂ concentration of 0.05 vol % or more and 30.0 vol % or less and a dew point of 0° C. or lower. The first heating process is performed to form a microstructure including bainite as a main phase with austenite or martensite being included as part of the microstructure.

Since it is necessary that the H₂ concentration be sufficient for inhibiting oxidation of Fe, the H₂ concentration is set to be 0.05 vol % or more. On the other hand, in the case where the H₂ concentration is more than 30.0 vol %, there is an increase in cost. Therefore, the H₂ concentration is set to be 30.0 vol % or less. The remaining constituents of the atmosphere gas in the first heating process are N₂, H₂O, and inevitable impurities.

In addition, in the case where the dew point of the atmosphere in the first heating process is higher than 0° C., oxidation of Fe occurs. Therefore, it is necessary that the dew point be 0° C. or lower. Here, although there is no particular limitation on the lower limit of the dew point, it is preferable that the dew point be −60° C. or higher, because it is difficult to achieve a dew point of lower than −60° C. industrially.

In the case where the temperature of the steel sheet is lower than 800° C., since there is a decrease in the austenite phase fraction when the heat treatment is performed, C and Mn are inhomogeneously distributed in the microstructure, which may make it impossible to achieve an excellent strength-elongation balance due to an inhomogeneous microstructure being formed in the subsequent processes. On the other hand, in the case where the temperature of the steel sheet is higher than 950° C., there is an excessive increase in austenite grain diameter, which may finally make it impossible to achieve an excellent TS-El balance. Therefore, the heating temperature of the steel sheet to be held (steel sheet temperature) is set to be 800° C. or higher and 950° C. or lower. In the first heating process, the steel sheet may be held at a constant temperature, or the temperature may vary within the temperature range of 800° C. or higher and 950° C. or lower.

First Pickling Process

The surface of the steel sheet which has been subjected to the first heating process is pickled in an oxidizing acidic aqueous solution, and the pickled surface is rinsed in water. This first pickling process is performed for the purpose of cleaning the surface of the steel sheet, removing Si-based oxides, which have been formed on the surface of the steel sheet in the first heating process, and forming fine asperity on the surface of the steel sheet. Generally, since Si oxides have low solubility in acid, it takes a long time to completely dissolved and remove Si oxides. Therefore, using an oxidizing strong acid, such as nitric acid, as a pickling solution to remove Si oxides along with the base steel in the surface layer of the steel sheet is effective. At this time, since fine asperity is formed on the surface of the steel sheet as a result of the base steel being dissolved, there is an improvement in coating adhesiveness due to an anchor effect at the final coating interface. Examples of an oxidizing acidic aqueous solution include nitric acid, which is an oxidizing strong acid. Also, a mixture of nitric acid and at least one of hydrochloric acid, hydrofluoric acid, and sulfuric acid, which are non-oxidizing strong acids, may be used. In addition, in the case where an oxidizing acidic aqueous solution is used, it is preferable that the temperature be 20° C. to 70° C. and that the pickling time be 3 seconds to 30 seconds.

In addition, it is necessary to rapidly rinse the pickled steel sheet in water. In the case where rinsing in water is not performed, large amounts of Fe-based oxides and Fe-based hydroxides are inhomogeneously formed on the surface of the steel sheet due to the oxidizing power of the acidic solution remaining on the surface of the steel sheet, which may result in uneven surface appearance.

Second Pickling Process

The second pickling process is a process in which the surface of the steel sheet which has been subjected to the first pickling process is pickled again. This process is performed for the purpose of removing the Fe-based oxides and the Fe-based hydroxides, which have been formed on the surface of the steel sheet which has been subjected to the first pickling process, and of completely removing Si-based oxides, which may be remaining in a small amount on the surface of the steel sheet. Here, the Fe-based oxides and the Fe-based hydroxides are formed as a result of the base steel being oxidized by the pickling solution in the first pickling process. Therefore, it is necessary to use a non-oxidizing acidic aqueous solution in the second pickling process so that Fe-based oxides and Fe-based hydroxides are prevented from being formed again after the second pickling process has been performed. Examples of a preferable non-oxidizing acidic aqueous solution include a mixture of one, two, or more selected from hydrochloric acid, sulfuric acid, phosphoric acid, pyrophosphoric acid, formic acid, acetic acid, citric acid, hydrofluoric acid, and oxalic acid.

Here, regardless of the acids selected for the mixture described above, it is preferable that the temperature be 20° C. to 70° C. and that the pickling time be 1 second to 30 seconds.

In addition, it is necessary to rapidly rinse the pickled steel sheet in water. In the case where rinsing in water is not performed, the remaining pickling solution forms inhomogeneous asperity and corrosion products on the surface of the steel sheet, which may result in a deterioration in final surface appearance.

Second Heating Process

The steel sheet which has been subjected to the second pickling process is held in a temperature range of 700° C. or higher and 900° C. or lower in an atmosphere having a H₂ concentration of 0.05 vol % or more and 30.0 vol % or less and a dew point of 0° C. or lower for 20 seconds or more and 300 seconds or less. The second heating process is performed for the purpose of forming the final microstructure and activating the surface of the steel sheet before the steel sheet is subjected to a galvanizing treatment.

Since it is necessary that the H₂ concentration be sufficient for inhibiting oxidation of Fe, the H₂ concentration is set to be 0.05 vol % or more. In addition, in the case where the H₂ concentration is more than 30.0 vol %, there is an increase in cost. Therefore, the H₂ concentration is set to be 30.0 vol % or less. The remaining constituents are N₂, H₂O, and inevitable impurities.

In addition, in the case where the dew point is higher than 0° C., since Fe is hard to be reduced, it is not possible to clean the surface of the steel sheet before a galvanizing treatment is performed, which may result in a deterioration in coating wettability. Therefore, the dew point is set to be 0° C. or lower.

In the case where the steel sheet temperature is lower than 700° C., since there is an excessive increase in the amount of a ferrite phase during the heat treatment, there may be a case where it is not possible to achieve an excellent strength-elongation balance. Moreover, since the surface of the steel sheet is not sufficiently activated due to, for example, a natural oxide film on the surface of the steel sheet not being sufficiently reduced, there is a deterioration in wettability with molten zinc. On the other hand, in the case where the steel sheet temperature is higher than 900° C., since there is an excessive increase in the amount of an austenite phase during the heat treatment, there may be a case where it is not possible to achieve an excellent strength-elongation balance. Moreover, since a large amount of Si-based oxides is formed on the surface of the steel sheet during annealing, there is a deterioration in wettability between the steel sheet and molten zinc when a galvanizing treatment is performed. Therefore, the temperature at which the steel sheet is held in the second heating process is set to be 700° C. or higher and 900° C. or lower. Here, the holding temperature may remain constant or vary as long as the temperature is within the range described above.

In addition, in the case where the holding time is less than 20 seconds, since, for example, a natural oxide film on the surface of the steel sheet is not sufficiently reduced, there may be a case where the surface of the steel sheet is not sufficiently activated before a galvanizing treatment is performed. On the other hand, in the case where the holding time is more than 300 seconds, since a large amount of Si-based oxides are formed on the surface of the steel sheet, there is a deterioration in wettability between the steel sheet and molten zinc when a galvanizing treatment is performed. Therefore, the holding time is set to be 20 seconds or more and 300 seconds or less.

In addition, the steel sheet may be subjected to an oxidizing process and a reducing process as needed after the second pickling process and before the second heating process. Hereafter, the oxidizing process and the reducing process will be described.

Oxidizing Process

The oxidizing process is performed for the purpose of forming an Fe oxide film on the surface of the steel sheet to inhibit Si surface oxides and Mn surface oxides from being formed when reducing annealing is performed in the subsequent second heating process.

To oxidize Fe, it is preferable that the O₂ concentration be 0.1 vol % or more. On the other hand, it is preferable that the O₂ concentration be 20 vol % or less, which is the same level as the air, from the viewpoint of cost saving. In addition, to promote oxidation of Fe, it is preferable that the H₂O concentration be 1 vol % or more. On the other hand, it is preferable that the H₂O concentration be 50 vol % or less for economic reasons. Moreover, even in an atmosphere satisfying the requirements described above, Fe is not sufficiently oxidized in the case where the heating temperature, at which the steel sheet is heated, is lower than 400° C. On the other hand, in the case where the steel sheet temperature is higher than 900° C., since there is an excessive increase in the amount of Fe oxidized, a pickup defect of iron oxides occurs in rolls and unreduced Fe remains in the second heating process, which may result in a deterioration, rather than improvement, in surface appearance and coating adhesiveness after galvanizing treatment. Therefore, it is preferable that the steel sheet temperature be 400° C. or higher and 900° C. or lower.

Reducing Process

The reducing process is performed for the purpose of reducing the Fe oxide film, to such an extent that Fe oxide is not separated, to prevent the steel sheet which has been subjected to the oxidizing process from causing a pickup defect to occur in rolls in the second heating process.

To form reduced Fe, it is preferable that the O₂ concentration be less than 0.1 vol %. However, it is preferable that the O₂ concentration be 0.01 vol % or more. In addition, it is also preferable that the H₂O concentration be 20 vol % or less to prevent oxidation of Fe. However, it is preferable that the H₂O concentration be 1 vol % or more. In addition, reduced Fe is hard to be formed in the case where the steel sheet temperature is lower than 600° C., and there is an economic disadvantage due to an increase in heating costs in the case where the temperature is higher than 900° C. Therefore, it is preferable that the steel sheet temperature be 600° C. or higher and 900° C. or lower.

Process of Performing Galvanizing Treatment

The process of performing a galvanizing treatment is a process in which the steel sheet which has been subjected to the processes described above is cooled and dipped in a galvanizing bath to perform a galvanizing treatment.

To manufacture a galvanized steel sheet, it is preferable that a galvanizing bath having a temperature of 440° C. to 550° C. and an Al concentration in the bath of 0.13% to 0.24% be used.

In the case where the bath temperature is lower than 440° C., Zn may be solidified in a low-temperature zone which is formed due to a variation in temperature in the bath, which is inappropriate for a hot-dip plating bath. In the case where the bath temperature is higher than 550° C., since there is a significant vapor generation from the bath, the vaporized Zn adheres to the interior of the line, which may cause difficulties in operation. In addition, alloying progresses when galvanizing treatment is performed, which may result in an excessive increase in alloying degree.

In the case where the Al concentration in the bath is less than 0.13% when a galvanized steel sheet is manufactured, since there is an increase in the degree of Fe—Zn alloying, there may be a case of a deterioration in coating adhesiveness. In the case where the Al concentration is more than 0.24%, defects caused by Al oxides may occur.

In the case where an alloying treatment is performed after the galvanizing treatment has been performed, it is preferable that a galvanizing bath having an Al concentration of 0.10% to 0.20% be used. In the case where the Al concentration in the bath is less than 0.10%, since a large amount of F phase is formed, there may be a case of a deterioration in coating adhesiveness. In the case where the Al concentration is more than 0.20%, there may be a case where Fe—Zn alloying does not progress.

Alloying Treatment Process

The steel sheet which has been subjected to a galvanizing treatment process is further subjected to an alloying treatment as needed. Although there is no particular limitation on the conditions applied for the alloying treatment, it is preferable that the alloying treatment temperature be higher than 460° C. and lower than 600° C. In the case where the alloying temperature is 460° C. or lower, since alloying progresses at a low rate, it takes a long time to sufficiently perform alloying treatment, which results in a decrease in efficiency. In the case where the alloying temperature is 600° C. or higher, since there is an excessive increase in alloying degree, an excessive amount of hard and brittle Zn—Fe-alloy layer is formed at the base steel interface, which may result in a deterioration in coating adhesiveness.

EXAMPLES

Molten steels having the chemical compositions given in Table 1 with the balance being Fe and inevitable impurities were prepared and made into slabs. The obtained slabs were heated to a temperature of 1200° C., hot-rolled, and coiled. Subsequently, the obtained hot-rolled steel sheets were pickled and cold-rolled with a rolling reduction ratio of 50%. The obtained cold-rolled steel sheets were subjected to the first heating process, the first pickling process, the second pickling process, the second heating process, and the galvanizing treatment process under the conditions given in Table 2 and Table 3 in a furnace whose atmosphere was controllable. In the galvanizing treatment process, a galvanizing treatment was performed in a Zn bath having an Al concentration of 0.132%. In addition, some of the steel sheets were further subjected to an alloying treatment.

The tensile strength (TS), total elongation (EL), surface appearance, and coating adhesiveness (GI-adhesiveness and GA-adhesiveness) of the galvanized steel sheet (GI) and the galvannealed steel sheet (GA) obtained as described above were evaluated by using the methods described below.

<Tensile Strength and Total Elongation>

A tensile test was performed in accordance with JIS Z 2241 on a JIS No. 5 test piece which was taken from the steel sheet so that the tensile direction was perpendicular to the rolling direction to obtain TS (tensile strength) and total elongation (EL), and the level of elongation was evaluated in terms of the value of (TS)×(EL). In EXAMPLE, a case where (TS)×(EL) was 15000 MPa or more was determined as a case of good elongation.

<Surface Appearance>

Whether surface appearance defects, such as non-coating and a pinhole, existed was determined by performing visual observation. Evaluation was performed on the basis of the standard below, and a case of “B” or “C” was determined as preferable in the disclosed embodiments.

A: especially good without surface appearance defects B: good almost without surface appearance defects C: generally good with slight surface appearance defects D: with surface appearance defects

<Coating Adhesiveness>

The coating adhesiveness of the galvanized steel sheet (GI) was evaluated after having performed a ball impact test followed by a tape-peeling test on the worked portion. Whether coating layer separation occurred was determined by performing visual observation. The evaluation was performed on the basis of the standard below, and a case of “B” was determined as preferable. Here, the ball impact test was performed with a ball mass of 1.8 kg and a drop height of 100 cm.

B: No Coating Layer Separation, C: Slight Coating Layer Separation, D: Coating Layer Separation

The coating adhesiveness of the galvannealed steel sheet (GA) was evaluated by performing a test for evaluating powdering resistance. Specifically, after having performed a 90-degree bending-unbending test on the surface of the galvannealed steel sheet to which a cellophane tape was applied, a cellophane tape having a width of 24 mm was pressed onto the inner side (compression side) of the worked portion so that the tape was parallel to the bending worked portion, and the pressed tape was peeled. The amount of zinc which adhered to a portion having a length of 40 mm of the peeled cellophane tape was determined in terms of Zn count number obtained by performing X-ray fluorescence spectrometry, and the determined Zn count was converted into that per unit length (1 m), which was used in the ranking on the basis of the standard below. In the disclosed embodiments, a case of rank 1 was determined as especially good (A), a case of rank 2 was determined as good (B), a case of rank 3 was determined as generally good (C), a case of rank 4 or more was determined as poor (D), and a case of “A”, “B”, or “C” was determined as preferable.

Fluorescent X-Ray Count Number and Corresponding Rank

0 or more and less than 2000: 1 (good) 2000 or more and less than 5000: 2 5000 or more and less than 8000: 3 8000 or more and less than 10000: 4 10000 or more: 5 (poor)

The evaluation results obtained as described above are given in Tables 2 through 5 along with the conditions.

TABLE 1 (mass %) Steel Grade Code C Si Mn P S Al N Ti Nb B Mo A 0.136 1.56 2.15 0.006 0.0013 0.040 0.0035 — — — — B 0.177 1.91 2.24 0.003 0.0015 0.015 0.0029 0.021 0.035 0.0014 — C 0.129 0.85 2.79 0.005 0.0013 0.033 0.0038 0.032 — — — D 0.184 1.51 2.83 0.005 0.0012 0.032 0.0023 0.043 0.051 — 0.021 E 0.129 1.67 1.02 0.009 0.0010 0.034 0.0032 0.023 0.032 — — F 0.110 1.20 2.50 0.008 0.0012 0.021 0.0031 — — — — G 0.119 1.12 2.04 0.008 0.0010 0.028 0.0028 — — — — H 0.152 1.15 1.92 0.006 0.0011 0.025 0.0021 — — — — I 0.138 1.32 1.50 0.009 0.0010 0.032 0.0011 — — — — J 0.210 1.72 1.77 0.003 0.0010 0.015 0.0016 — — — — K 0.193 1.37 2.55 0.007 0.0012 0.029 0.0019 — — — — L 0.143 1.08 2.12 0.005 0.0013 0.024 0.0027 — — — — M 0.136 1.49 4.16 0.007 0.0009 0.021 0.0024 0.042 0.019 — — N 0.112 2.43 1.89 0.004 0.0008 0.028 0.0034 0.029 0.031 0.0012 — O 0.114 0.70 1.89 0.004 0.0008 0.028 0.0034 — — — — (mass %) Steel Grade Code Cr Ni Cu V Sb Sn Ca REM Note A — — — — — — — — Example Steel B — — — — — — — — Example Steel C — — — — — — — — Example Steel D — — — — — — — — Example Steel E 0.12 — — — — — — — Example Steel F — — 0.09 — — — — — Example Steel G — 0.14 — — — — — Example Steel H — — — — — 0.03 — — Example Steel I — — — — 0.06 — — — Example Steel J — — — — — — 0.004 — Example Steel K — — — 0.0700 — — — — Example Steel L — — — — — — — 0.005 Example Steel M — — — — — — — — Comparative Steel N — — — — — — — — Comparative Steel O — — — — — — — — Comparative Steel

TABLE 2 First Heating Process Oxidizing Process Reducing Process Heating First Pickling Second Pickling Heating Heating Dew Temper- Process Process Temper- Temper- H₂ point ature Pickling Pickling Pickling Pickling O₂ H₂O ature O₂ H₂O ature No Steel (%) (° C.) (° C.) Solution Time (s) Solution Time (s) (%) (%) (° C.) (%) (%) (° C.) 1 A 10.0 −35 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 2 A 10.0 −35 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 3 A 25.0 −30 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 4 A 0.1 −30 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 5 A 10.0 0 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 6 A 10.0 −45 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 7 A 10.0 −35 950 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 8 A 10.0 −35 800 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 9 A 10.0 −35 860 150 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid Hydrochloric Acid 10 A 10.0 −35 860 150 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrofluoric Acid 11 A 10.0 −35 860 120 g/L 10.0 30 g/L 5.0 — — — — — — Nitric Acid + Sulfuric 20 g/L Acid Hydrochloric Acid 12 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrofluoric 20 g/L Acid Hydrochloric Acid 13 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 14 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 15 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 16 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 17 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 18 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 19 B 10.0 −35 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 20 B 10.0 −35 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 21 B 10.0 −35 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 22 B 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 23 B 0.1 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 24 B 10.0 −5 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 25 B 10.0 −35 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 26 B 10.0 −35 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 27 B 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 28 B 10.0 −40 860 150 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid Hydrochloric Acid 29 B 10.0 −40 860 150 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 30 g/L Acid Sulfuric Acid 30 B 10.0 −40 860 120 g/L 10.0 30 g/L 5.0 — — — — — — Nitric Acid + Sulfuric 20 g/L Acid Hydrochloric Acid 31 B 10.0 −35 950 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 32 B 10.0 −35 800 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 33 B 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 34 C 10.0 −10 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 35 C 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 36 C 0.1 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 37 C 10.0 −40 860 150 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid Hydrochloric Acid 38 C 10.0 −40 950 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 39 C 10.0 −40 800 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 40 C 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 41 C 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 42 C 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 43 C 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 44 C 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 45 C 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 46 D 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 47 D 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 48 D 0.1 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 49 D 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 50 E 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid +20 g/L Hydrochloric Hydrochloric Acid Acid 51 E 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 52 E 10.0 −40 950 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 53 F 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 54 F 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 55 G 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 56 G 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 57 H 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 58 I 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 59 J 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 60 K 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 61 L 10.0 −40 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid Alloying Second Heating Process Treatment Heating Process TS × Ra after Dew Temper- Holding Alloying EL Coating H₂ point ature Time Temperature (MPa · Separation Surface GI GA No Steel (%) (° C.) (° C.) (s) (° C.) %) (μm) Appearance Adhesiveness Adhesiveness Note 1 A 10.0 −40 800 150 — 15150 1.0 B C — Example 2 A 10.0 −40 800 150 560 15150 0.8 B — B Example 3 A 10.0 −35 800 150 560 16891 1.1 B — B Example 4 A 10.0 −35 800 150 560 20755 0.6 B — B Example 5 A 10.0 −35 800 150 560 17160 0.9 B — B Example 6 A 10.0 −35 800 150 560 17723 0.8 B — B Example 7 A 10.0 −35 800 150 560 19110 1.0 B — B Example 8 A 10.0 −35 800 150 560 18514 0.6 B — B Example 9 A 10.0 −35 800 150 560 21124 0.9 B — B Example 10 A 10.0 −35 800 150 560 17328 0.8 B — B Example 11 A 10.0 −40 820 150 560 17398 1.7 B — B Example 12 A 10.0 −35 800 150 560 19572 0.6 B — B Example 13 A 0.05 −35 800 150 566 20641 1.4 B — B Example 14 A 27.0 −35 800 150 560 15283 1.1 B — B Example 15 A 10.0 −35 700 150 560 19145 0.8 A — B Example 16 A 10.0 −35 900 150 560 17030 1.5 B — B Example 17 A 10.0 −3 800 150 560 17159 1.7 B — B Example 18 A 10.0 −50 800 150 560 19296 1.1 A — A Example 19 B 10.0 −30 760 25 — 21150 0.6 B B — Example 20 B 10.0 −30 760 150 — 21037 1.0 B B — Example 21 B 10.0 −30 760 300 — 20221 1.4 C C — Example 22 B 10.0 −30 760 150 — 21278 1.4 B B — Example 23 B 10.0 −30 760 150 — 19758 0.6 C B — Example 24 B 10.0 −30 760 150 — 19254 1.9 B B — Example 25 B 10.0 −30 900 150 — 16812 0.6 C C — Example 26 B 10.0 −30 720 150 — 15772 1.7 C C — Example 27 B 10.0 −10 820 150 530 18364 1.9 A — B Example 28 B 10.0 −30 760 150 — 18981 1.1 B B — Example 29 B 10.0 −30 760 150 — 21290 1.5 B B — Example 30 B 10.0 −30 760 150 — 16115 0.8 B B — Example 31 B 10.0 −30 760 150 — 15391 0.9 B B — Example 32 B 10.0 −30 760 150 — 15527 1.1 B B — Example 33 B 0.1 −30 760 150 — 20991 1.4 B B — Example 34 C 10.0 −35 810 150 550 18340 1.5 B — B Example 35 C 10.0 −35 810 150 550 20806 0.7 B — B Example 36 C 10.0 −35 810 150 550 15613 0.9 B — B Example 37 C 10.0 −35 810 150 550 17848 1.6 B — B Example 38 C 10.0 −35 810 150 550 20914 1.3 B — B Example 39 C 10.0 −35 810 150 550 16567 0.8 B — B Example 40 C 10.0 −45 810 150 — 18173 1.1 A A — Example 41 C 10.0 −20 800 150 — 15573 1.5 B B — Example 42 C 10.0 −40 820 300 550 19031 0.7 C — B Example 43 C 0.1 −35 810 150 — 21481 1.8 B B — Example 44 C 10.0 −35 700 150 550 19911 1.4 B — C Example 45 C 10.0 −35 900 150 550 18810 1.7 B — B Example 46 D 10.0 −40 800 150 — 19262 1.1 B B — Example 47 D 10.0 −20 820 150 530 18467 1.7 B — A Example 48 D 10.0 −40 800 150 — 18116 1.2 C B — Example 49 D 10.0 −45 820 150 530 20527 1.1 B — A Example 50 E 10.0 −40 800 150 — 20640 1.4 C — — Example 51 E 10.0 −50 800 150 550 16861 1.2 A — B Example 52 E 10.0 −40 800 150 550 16754 1.6 B — B Example 53 F 10.0 −40 820 150 520 18759 1.6 B — B Example 54 F 10.0 −45 820 150 520 19550 1.9 A — B Example 55 G 10.0 −40 850 150 550 15461 1.4 B — B Example 56 G 10.0 −5 850 150 550 17784 1.2 B — B Example 57 H 10.0 −40 820 150 560 20815 1.1 B — B Example 58 I 10.0 −40 850 150 — 21254 0.6 B B — Example 59 J 10.0 −40 850 150 — 16210 1.7 C C — Example 60 K 10.0 −40 850 150 — 21252 0.8 B B — Example 61 L 10.0 −40 850 150 — 21458 1.3 B B — Example

TABLE 3 First Heating Process Oxidizing Process Reducing Process Heating First Pickling Second Pickling Heating Heating Dew Temper- Process Precess Temper- Temper- H₂ point ature Pickling Pickling Pickling Pickling O₂ H₂O ature O₂ H₂O ature No Steel (%) (° C.) (° C.) Solution Time (s) Solution Time (s) (%) (%) (° C.) (%) (%) (° C.) 62 A 10.0 −35 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 63 A 0.01 −35 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 64 A 10.0 5 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 65 A 10.0 −35 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 66 A 10.0 −35 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 67 A 10.0 −35 860 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 68 A 10.0 −35 850 — — — — — — — — — — 69 A 10.0 −40 750 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 70 A 10.0 −30 980 140 g/L 10.0 25 g/L 5.0 — — — — — — Hydrochloric Hydrochloric Acid Acid 71 A 10.0 −30 860 140 g/L 10.0 25 g/L 5.0 — — — — — — Hydrochloric Hydrochloric Acid Acid 72 B 10.0 −30 850 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Nitric Acid 20 g/L Hydrochloric Acid 73 B 10.0 −30 850 120 g/L 10.0 — — — — — — — — Nitric Acid + 20 g/L Hydrochloric Acid 74 M 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 75 N 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 76 O 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 — — — — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid Alloying Second Heating Process Treatment Heating Process TS × Ra after Dew Temper- Holding Alloying EL Coating H₂ point ature Time Temperature (MPa · Separation Surface GI GA No Steel (%) (° C.) (° C.) (s) (° C.) %) (μm) Appearance Adhesiveness Adhesiveness Note 62 A 15.0 −40 950 150 560 14200 1.1 D — D Comparative Example 63 A 15.0 −40 800 150 560 17294 1.2 B — D Comparative Example 64 A 15.0 −40 800 150 560 17664 0.7 D — D Comparative Example 65 A 0.01 −40 800 150 560 16006 1.1 D — D Comparative Example 66 A 15.0 10 800 150 560 16405 1.5 D — D Comparative Example 67 A 15.0 −40 650 150 560 13850 1.5 D — D Comparative Example 68 A 15.0 −30 800 160 530 16031 0.2 D — D Comparative Example 69 A 10.0 −40 800 150 — 14050 1.3 A B — Comparative Example 70 A 10.0 −35 850 180 560 12950 0.5 D — D Comparative Example 71 A 10.0 −35 850 180 560 15987 0.5 D — D Comparative Example 72 B 15.0 −45 850 160 — 18246 2.3 B D — Comparative Example 73 B 15.0 −45 850 160 — 16843 0.8 C D — Comparative Example 74 M 15.0 −40 820 160 — 17975 1.1 D D — Comparative Example 75 N 15.0 −35 820 160 — 21629 0.9 D B — Comparative Example 76 O 15.0 −35 820 160 530 13200 1.9 B — B Comparative Example

TABLE 4 First Heating Process Oxidizing Process Reducing Process Heating First Pickling Second Pickling Heating Heating Dew Temper- Process Precess Temper- Temper- H₂ point ature Pickling Pickling Pickling Pickling O₂ H₂O ature O₂ H₂O ature No Steel (%) (° C.) (° C.) Solution Time (s) Solution Time (s) (%) (%) (° C.) (%) (%) (° C.) 77 A 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 78 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 79 A 28.0 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 80 A 0.07 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 81 A 10.0 0 860 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 82 A 10.0 −45 860 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 83 A 10.0 −35 950 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 84 A 10.0 −35 800 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 85 A 10.0 −35 860 150 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 750 Nitric Acid Hydrochloric Acid 86 A 10.0 −35 860 120 g/L 10.0 30 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Sulfuric Acid 20 g/L Hydrochloric Acid 87 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 88 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 89 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 90 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 91 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 92 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 20.0 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 93 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 0.1 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 94 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 50 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 95 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 1.0 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 96 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 15 400 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 97 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 15 880 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 98 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.08 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 99 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 1.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 100 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 19.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 101 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 600 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 102 A 10.0 −30 860 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 900 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 103 B 15.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 — — — Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 104 B 15.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 105 B 15.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 106 B 15.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 107 B 10.0 −40 810 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 108 C 5.0 −35 800 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 109 C 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 110 C 5.0 −40 820 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5.0 750 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 111 C 10.0 −30 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 112 D 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 113 D 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 114 E 5.0 −40 820 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 115 E 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 116 F 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 117 G 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 118 H 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 119 I 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 120 J 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 121 K 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 122 L 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5.0 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid Alloying Second Heating Process Treatment Heating Process TS × Ra after Dew Temper- Holding Alloying EL Coating H₂ point ature Time Temperature (MPa · Separation Surface GI GA No Steel (%) (° C.) (° C.) (s) (° C.) %) (μm) Appearance Adhesiveness Adhesiveness Note 77 A 15.0 −40 820 160 — 16408 1.2 A B — Example 78 A 10.0 −35 800 180 560 20611 1.5 A — B Example 79 A 10.0 −35 800 180 560 17178 0.7 A — B Example 80 A 10.0 −35 800 180 560 15108 1.5 A — B Example 81 A 10.0 −35 800 180 560 21792 1.1 B — B Example 82 A 10.0 −35 800 180 560 17279 1.7 A — B Example 83 A 10.0 −35 800 180 560 19839 1.6 B — B Example 84 A 10.0 −35 800 180 560 21470 1.5 B — B Example 85 A 10.0 −35 800 180 560 15776 1.9 B — B Example 86 A 15.0 −40 820 160 560 19893 1.3 B — B Example 87 A 0.05 −35 800 180 560 21568 1.4 A — B Example 88 A 28.0 −35 800 180 560 18206 1.2 A — B Example 89 A 10.0 −35 700 180 560 20811 1.5 A — B Example 90 A 10.0 −35 900 180 560 21004 0.6 B — B Example 91 A 10.0 −5 800 180 560 20684 1.6 A — A Example 92 A 10.0 −35 800 180 560 18338 1.9 B — B Example 93 A 10.0 −35 800 180 560 15427 1.8 C — B Example 94 A 10.0 −35 800 180 560 15524 1.6 C — A Example 95 A 10.0 −35 800 180 560 16359 0.8 B — B Example 96 A 10.0 −35 800 180 560 21345 1.0 B — B Example 97 A 10.0 −35 800 180 560 18337 1.6 A — B Example 98 A 10.0 −35 800 180 560 21180 1.2 B — B Example 99 A 10.0 −35 800 180 560 17700 1.5 B — B Example 100 A 10.0 −35 800 180 560 16941 1.5 B — B Example 101 A 10.0 −35 800 180 560 21590 0.7 B — B Example 102 A 10.0 −35 800 180 560 19414 1.6 B — B Example 103 B 15.0 −30 760 160 — 21922 1.5 A B — Example 104 B 15.0 −30 760 30 — 17061 0.8 B A — Example 105 B 15.0 −30 760 300 — 18615 0.6 A B — Example 106 B 15.0 −30 760 160 — 19524 1.4 A B — Example 107 B 10. −10 820 150 530 20730 1.3 A — A Example 108 C 10. −35 810 160 550 17258 1.4 B — B Example 109 C 10. −40 790 160 — 17767 1.8 B B — Example 110 C 15.0 −30 800 160 — 15680 1.2 A B — Example 111 C 15.0 −40 820 160 550 15999 1.6 B — B Example 112 D 10.0 −40 800 160 — 19588 1.5 B B — Example 113 D 15.0 −20 820 160 530 19782 1.9 A — A Example 114 E 15.0 −40 800 160 — 16949 1.6 B B — Example 115 E 15.0 −40 800 160 550 17313 1.6 B — B Example 116 F 15.0 −40 820 160 520 19195 0.8 B — B Example 117 G 15.0 −40 850 160 550 20288 0.8 B — B Example 118 H 15.0 −40 820 160 560 15549 1.2 B — B Example 119 I 15.0 −40 850 160 — 20889 1.3 B B — Example 120 J 15.0 −40 850 160 — 19894 1.7 B B — Example 121 K 15.0 −40 850 160 — 20842 1.8 B B — Example 122 L 15.0 −40 850 160 — 19060 1.6 B B — Example

TABLE 5 First Heating Process Oxidizing Process Reducing Process Heating First Pickling Second Pickling Heating Heating Dew Temper- Process Process Temper- Temper- H₂ point ature Pickling Pickling Pickling Pickling O₂ H₂O ature O₂ H₂O ature No Steel (%) (° C.) (° C.) Solution Time (s) Solution Time (s) (%) (%) (° C.) (%) (%) (° C.) 123 A 10.0 −35 860 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 124 A 0.01 −35 860 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 125 A 10.0 10 860 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 126 A 10.0 −35 860 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 127 A 10.0 −35 860 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 128 A 10.0 −35 860 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 129 A 10.0 −40 850 — — — — 1.0 15 650 0.01 5 700 130 A 10.0 −40 750 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 131 A 10.0 −40 980 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 132 A 10.0 −30 860 140 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5 750 Hydrochloric Hydrochloric Acid Acid 133 B 10.0 −30 850 120 g/L 10.0 25 g/L 5.0 1.0 15 700 0.01 5 750 Nitric Acid + Nitric Acid 20 g/L Hydrochloric Acid 134 B 10.0 −30 850 120 g/L 10.0 — — 1.0 15 700 0.01 5 750 Nitric Acid + 20 g/L Hydrochloric Acid 135 M 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 136 N 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid 137 O 10.0 −40 850 120 g/L 10.0 25 g/L 5.0 1.0 15 650 0.01 5 700 Nitric Acid + Hydrochloric 20 g/L Acid Hydrochloric Acid Alloying Second Heating Process Treatment Heating Process TS × Ra after Dew Temper- Alloying EL Coating H₂ point ature Holding Temperature (MPa · Separation Surface GI GA No Steel (%) (° C.) (° C.) Time (s) (° C.) %) (μm) Appearance Adhesiveness Adhesiveness Note 123 A 15.0 −40 950 150 560 13900 0.6 D — D Comparative Example 124 A 15.0 −40 800 150 560 16263 1.3 C — D Comparative Example 125 A 15.0 −40 800 150 560 20512 1.9 D — D Comparative Example 126 A 0.01 −40 800 150 560 16263 1.4 D — D Comparative Example 127 A 15.0 10 800 150 560 16263 1.9 D — D Comparative Example 128 A 15.0 −40 680 150 560 14060 1.3 D — D Comparative Example 129 A 15.0 −30 850 160 530 16660 0.2 D — D Comparative Example 130 A 10.0 −35 810 150 — 13800 1.9 A B — Comparative Example 131 A 10.0 −35 810 150 — 14190 1.9 A B — Comparative Example 132 A 10.0 −35 800 180 560 17200 0.5 D — D Comparative Example 133 B 15.0 −45 820 160 — 19846 2.3 D D — Comparative Example 134 B 15.0 −45 820 160 — 16895 0.8 D D — Comparative Example 135 M 15.0 −40 820 160 — 19806 1.5 D C — Comparative Example 136 N 15.0 −35 820 160 — 20970 1.8 D C — Comparative Example 137 O 15.0 −35 820 160 530 12100 0.6 A — B Comparative Example

It is clarified that all the high-strength galvanized steel sheets of the examples were excellent in terms of elongation, surface appearance, and coating adhesiveness. In contrast, the comparative examples were poor in terms of at least one of elongation, surface appearance, and coating adhesiveness. 

1. A method for manufacturing a high-strength galvanized steel sheet, the method comprising: a first heating process including heating a steel sheet to a temperature in a range of 800° C. or higher and 950° C. or lower in an atmosphere having a H₂ concentration of 0.05 vol % or more and 30.0 vol % or less and a dew point of 0° C. or lower, the steel sheet having a chemical composition comprising, by mass %: C: 0.040% or more and 0.500% or less, Si: 0.80% or more and 2.00% or less, Mn: 1.00% or more and 4.00% or less, P: 0.100% or less, S: 0.0100% or less, Al: 0.100% or less, N: 0.0100% or less, and a balance being Fe and inevitable impurities, a first pickling process including: (i) pickling the steel sheet which has been subjected to the first heating process, in an oxidizing acidic aqueous solution and (ii) rinsing the pickled steel sheet in water, a second pickling process including: (i) pickling the steel sheet, which has been subjected to the first pickling process, in a non-oxidizing acidic aqueous solution and (ii) rinsing the pickled steel sheet in water, a second heating process including holding the steel sheet which has been subjected to the second pickling process, at a temperature in a range of 700° C. or higher and 900° C. or lower in an atmosphere having a H₂ concentration of 0.05 vol % or more and 30.0 vol % or less and a dew point of 0° C. or lower for 20 seconds or more and 300 seconds or less, and performing a galvanizing treatment on the steel sheet which has been subjected to the second heating process.
 2. The method for manufacturing a high-strength galvanized steel sheet according to claim 1, wherein the chemical composition further comprises, by mass %, at least one selected from the group consisting of: Ti: 0.010% or more and 0.100% or less, Nb: 0.010% or more and 0.100% or less, and B: 0.0001% or more and 0.0050% or less.
 3. The method for manufacturing a high-strength galvanized steel sheet according to claim 1, wherein the chemical composition further comprises, by mass %, at least one selected from the group consisting of: Mo: 0.01% or more and 0.50% or less, Cr: 0.60% or less, Ni: 0.50% or less, Cu: 1.00% or less, V: 0.500% or less, Sb: 0.10% or less, Sn: 0.10% or less, Ca: 0.0100% or less, and REM: 0.010% or less.
 4. The method for manufacturing a high-strength galvanized steel sheet according to claim 1, further comprising an oxidizing process including heating the steel sheet to a temperature in a range of 400° C. or higher and 900° C. or lower in an atmosphere having an O₂ concentration of 0.1 vol % or more and 20 vol % or less and a H₂O concentration of 1 vol % or more and 50 vol % or less after the second pickling process and before the second heating process.
 5. The method for manufacturing a high-strength galvanized steel sheet according to claim 4, further comprising a reducing process including heating the steel sheet to a temperature in a range of 600° C. or higher and 900° C. or lower in an atmosphere having an O₂ concentration of 0.01 vol % or more and less than 0.1 vol % and a H₂O concentration of 1 vol % or more and 20 vol % or less after the oxidizing process.
 6. The method for manufacturing a high-strength galvanized steel sheet according to claim 1, wherein the oxidizing acidic aqueous solution in the first pickling process is: (i) nitric acid or (ii) a mixture of nitric acid and at least one selected from the group consisting of hydrochloric acid, hydrofluoric acid, and sulfuric acid.
 7. The method for manufacturing a high-strength galvanized steel sheet according to claim 1, wherein the non-oxidizing acidic aqueous solution in the second pickling process is at least one selected from the group consisting of hydrochloric acid, sulfuric acid, phosphoric acid, pyrophosphoric acid, formic acid, acetic acid, citric acid, hydrofluoric acid, and oxalic acid.
 8. The method for manufacturing a high-strength galvanized steel sheet according to claim 1, further comprising an alloying treatment process including performing an alloying treatment on the steel sheet which has been subjected to the galvanizing treatment.
 9. The method for manufacturing a high-strength galvanized steel sheet according to claim 2, wherein the chemical composition further comprises, by mass %, at least one selected from the group consisting of: Mo: 0.01% or more and 0.50% or less, Cr: 0.60% or less, Ni: 0.50% or less, Cu: 1.00% or less, V: 0.500% or less, Sb: 0.10% or less, Sn: 0.10% or less, Ca: 0.0100% or less, and REM: 0.010% or less.
 10. The method for manufacturing a high-strength galvanized steel sheet according to claim 2, further comprising an oxidizing process including heating the steel sheet to a temperature in a range of 400° C. or higher and 900° C. or lower in an atmosphere having an O₂ concentration of 0.1 vol % or more and 20 vol % or less and a H₂O concentration of 1 vol % or more and 50 vol % or less after the second pickling process and before the second heating process.
 11. The method for manufacturing a high-strength galvanized steel sheet according to claim 3, further comprising an oxidizing process including heating the steel sheet to a temperature in a range of 400° C. or higher and 900° C. or lower in an atmosphere having an O₂ concentration of 0.1 vol % or more and 20 vol % or less and a H₂O concentration of 1 vol % or more and 50 vol % or less after the second pickling process and before the second heating process.
 12. The method for manufacturing a high-strength galvanized steel sheet according to claim 9, further comprising an oxidizing process including heating the steel sheet to a temperature in a range of 400° C. or higher and 900° C. or lower in an atmosphere having an O₂ concentration of 0.1 vol % or more and 20 vol % or less and a H₂O concentration of 1 vol % or more and 50 vol % or less after the second pickling process and before the second heating process.
 13. The method for manufacturing a high-strength galvanized steel sheet according to claim 2, wherein the oxidizing acidic aqueous solution in the first pickling process is: (i) nitric acid or (ii) a mixture of nitric acid and at least one selected from the group consisting of hydrochloric acid, hydrofluoric acid, and sulfuric acid.
 14. The method for manufacturing a high-strength galvanized steel sheet according to claim 3, wherein the oxidizing acidic aqueous solution in the first pickling process is: (i) nitric acid or (ii) a mixture of nitric acid and at least one selected from the group consisting of hydrochloric acid, hydrofluoric acid, and sulfuric acid.
 15. The method for manufacturing a high-strength galvanized steel sheet according to claim 9, wherein the oxidizing acidic aqueous solution in the first pickling process is: (i) nitric acid or (ii) a mixture of nitric acid and at least one selected from the group consisting of hydrochloric acid, hydrofluoric acid, and sulfuric acid.
 16. The method for manufacturing a high-strength galvanized steel sheet according to claim 2, wherein the non-oxidizing acidic aqueous solution in the second pickling process is at least one selected from the group consisting of hydrochloric acid, sulfuric acid, phosphoric acid, pyrophosphoric acid, formic acid, acetic acid, citric acid, hydrofluoric acid, and oxalic acid.
 17. The method for manufacturing a high-strength galvanized steel sheet according to claim 3, wherein the non-oxidizing acidic aqueous solution in the second pickling process is at least one selected from the group consisting of hydrochloric acid, sulfuric acid, phosphoric acid, pyrophosphoric acid, formic acid, acetic acid, citric acid, hydrofluoric acid, and oxalic acid.
 18. The method for manufacturing a high-strength galvanized steel sheet according to claim 9, wherein the non-oxidizing acidic aqueous solution in the second pickling process is at least one selected from the group consisting of hydrochloric acid, sulfuric acid, phosphoric acid, pyrophosphoric acid, formic acid, acetic acid, citric acid, hydrofluoric acid, and oxalic acid. 